Canonical Allele Identifier: CA271434
Gene: CREBBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3850497G>A , CM000678.2:g.3850497G>A GRCh38
NC_000016.9:g.3900498G>A , CM000678.1:g.3900498G>A GRCh37
NC_000016.8:g.3840499G>A NCBI36
NG_009873.1:g.34624C>T
NG_009873.2:g.35217C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.598C>T MANE Select ENSP00000262367.5:p.Gln200Ter
ENST00000262367.9:c.598C>T ENSP00000262367.5:p.Gln200Ter
ENST00000382070.7:c.598C>T ENSP00000371502.3:p.Gln200Ter
NM_001079846.1:c.598C>T NP_001073315.1:p.Gln200Ter
NM_004380.2:c.598C>T NP_004371.2:p.Gln200Ter
XM_005255124.3:c.598C>T XP_005255181.1:p.Gln200Ter
XM_005255125.3:c.598C>T XP_005255182.1:p.Gln200Ter
XM_006720848.2:c.598C>T XP_006720911.1:p.Gln200Ter
XM_011522380.1:c.544C>T XP_011520682.1:p.Gln182Ter
XM_011522382.1:c.598C>T XP_011520684.1:p.Gln200Ter
XM_005255124.4:c.598C>T XP_005255181.1:p.Gln200Ter
XM_005255125.4:c.598C>T XP_005255182.1:p.Gln200Ter
XM_006720848.3:c.598C>T XP_006720911.1:p.Gln200Ter
XM_011522382.3:c.598C>T XP_011520684.1:p.Gln200Ter
XM_017022944.1:c.598C>T XP_016878433.1:p.Gln200Ter
NM_004380.3:c.598C>T MANE Select NP_004371.2:p.Gln200Ter